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Anti-IL-36R Monoclonal Antibody and Use Thereof for Inflammatory Disease Treatment

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Summary

USPTO published patent application US20260098101A1 from QYUNS THERAPEUTICS CO., LTD. covering an anti-human interleukin 36 receptor (IL-36R) monoclonal antibody for inflammatory disease treatment. The application was filed on December 4, 2025. The antibody comprises six complementarity determining regions with amino acid sequences specified in the filing, and the applicant claims superior neutralizing activity compared to Spesolimab at the cellular level.

What changed

USPTO published patent application US20260098101A1 disclosing an anti-human IL-36R monoclonal antibody comprising three heavy chain CDR regions (CDR-H1, CDR-H2, CDR-H3) and three light chain CDR regions (CDR-L1, CDR-L2, CDR-L3) with amino acid sequences as shown in SEQ ID NO: 1 through SEQ ID NO: 6. The application claims the antibody has comparable binding affinity to human IL-36R but superior neutralizing activity compared to Spesolimab.\n\nThis is a patent application publication, not a granted patent. Pharmaceutical companies developing biologic therapeutics targeting the IL-36 pathway should monitor this application for potential freedom-to-operate implications. Patent prosecution will determine whether the claims are ultimately allowed. The application does not create compliance obligations but may inform competitive intelligence regarding antibody-based inflammatory disease therapeutics.

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Archived snapshot

Apr 11, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← USPTO Patent Applications

ANTI-HUMAN INTERLEUKIN 36 RECEPTOR MONOCLONAL ANTIBODY AND USE THEREOF

Application US20260098101A1 Kind: A1 Apr 09, 2026

Assignee

QYUNS THERAPEUTICS CO., LTD.

Inventors

Jiwan QIU, Wang LI, Yi ZHOU, Wei CHEN, Yong KONG, Huaiyao QIAO, Yiliang WU, Tao CHEN

Abstract

The present invention provides an anti-human interleukin 36 receptor (IL-36R) monoclonal antibody and a use thereof. The monoclonal antibody comprises three heavy chain complementarity determining regions CDR-H1, CDR-H2 and CDR-H3 and three light chain complementarity determining regions CDR-L1, CDR-L2 and CDR-L3, and the amino acid sequences of CDR-H1, CDR-H2, CDR-H3, CDR-L1, CDR-L2 and CDR-L3 are as shown in SEQ ID NO: 1 to SEQ ID NO: 6, respectively. Compared with Spesolimab, the monoclonal antibody has comparable binding affinity to human IL-36R, and the neutralizing activity of the monoclonal antibody at the cellular level is superior to that of Spesolimab.

CPC Classifications

C07K 16/2866 C07K 2317/24 C07K 2317/76 C07K 2317/92

Filing Date

2025-12-04

Application No.

19409040

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Last updated

Classification

Agency
USPTO
Published
April 9th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
US20260098101A1

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers Healthcare providers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Patent examination IP licensing Biologic development
Geographic scope
United States US

Taxonomy

Primary area
Intellectual Property
Operational domain
Legal
Topics
Pharmaceuticals Healthcare

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